Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 17:7285140 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_020336

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts, has 2506 individual genotypes and is mentioned in 2 citations.

Variation displays